The document discusses drug induced diseases (DIDs), which are unintended harmful effects caused by medications. DIDs can affect many organ systems and cause conditions like skin disorders, lung disease, gastrointestinal issues, and neurological or kidney problems. Common causes of DIDs include nonsteroidal anti-inflammatory drugs, antibiotics, anticancer drugs, and anticonvulsants. DIDs are diagnosed based on symptoms occurring after drug intake. Treatment involves stopping the causative medication and managing symptoms. Preventing DIDs requires informing doctors of medical histories and only taking drugs as prescribed. DIDs remain an important health issue requiring more comprehensive research.

1. International Journal of Pharmaceutical Research and Development
6
Drug induced diseases
Mahewashsana A Pathan1*
, Mahesh D Londhe2
, Dayanand R Jadhav3
1-3
Department of Pharmaceutics, SSJP R.P. College of Pharmacy, Osmanabad, Maharashtra, India
Abstract
The Indian pharmaceutical industry is valued at Rs. 90000 crore and is growing at a rate of 12-14% annually. Exports are growing at a
rate of 25% compound annual growth rate. The total exports of Pharma products is to extent of Rs. 40000 crore. India has also
emerged as a hub for the clinical trials and drug discovery and development. Further more and more drug entities are being introduced
which includes new chemical entities, Pharma products, vaccines, dosage forms, and new routes of administration and new therapeutic
claims of existing drug moieties. The safe use of medicines is perhaps the single most important criteria that any regulatory authority
within a given country has to ensure in order to protect the public health and the integrity of its health care system. Drug induced
disease is defined as the unintended effect of a drug that results in mortality or morbidity with symptoms sufficient to prompt a patient
to seek medical attention and/or to require hospitalization and may persist even after the offending drug has been withdrawn. Drug
induced diseases also called as iatrogenic diseases, are well known but least studied entity. In this review, we have collected the
information from review and research articles related to the drug induced diseases. This review is intended to aid the understanding of
some basic concepts regarding the drug induced diseases. This tends to provide information about the some commonly occurring drug
induced disorders, the drugs responsible for inducing disorders, their prevention and some of the treatments.
Keywords: drug induced diseases, adverse effect, unintended drug reactions
Introduction
A drug-induced disease is an unintended effect of a drug, which
results in mortality or morbidity with symptoms sufficient to
prompt a patient to seek medical attention and/or require
hospitalization. Drug-induced disease can result from
unanticipated or anticipated drug effects [1]
. Public and
professional concern about drug induced diseases first arose in
the late 19th. In 1922; there was an enquiry into the jaundice
associated with the use of SALVARSAN, an organic arsenical
used in the treatment of Syphilis. In 1937 in the USA, 107
people died from taking an elixir of sulfanilamide that contained
the solvent diethylene glycol. This led to the establishment of
the Food and Drug Administration (FDA), which was given the
task of enquiring into the safety of new drugs before allowing
them to be marketed. The major modern catastrophe that
changed professional and public opinion towards medicines was
the thalidomide tragedy. The thalidomide incident led to a
public outcry, to the institution all round the world of drug
regulatory authorities, to the development of a much more
sophisticated approach to the preclinical testing and clinical
evaluation of drugs before marketing, and to a greatly increased
awareness of adverse effect of drugs and methods of detecting
them. With the adverse reactions some drugs have been
withdrawn from use or for some the label has been changed. [1]
2. Types
Diseases caused by drugs or drug induced diseases can be either
predictable or unpredictable.
Predictable: Predictable effects are an extension of the normal
pharmacological effects of the drug. For example, blood
thinners (anticoagulant and anti-platelet drugs) that are used to
prevent clotting of blood can cause bleeding as a side effect.
Several anti-diabetes medications like insulin and sulfonylureas
can cause low blood glucose levels.
Unpredictable: On the other hand, unpredictable effects are
completely unrelated to the therapeutic effect of the drug. For
example, amiodarone, a drug used to treat abnormal heart
rhythms, can cause lung damage. Depending on their severity,
drug-induced diseases may be classified as mild, moderate,
severe, or lethal if they cause death [2]
. Drug-induced diseases
can affect various organ systems of the body. Several drugs
have been banned because of their ability to cause serious
diseases. here are some examples listed below according to the
organ system affected [2]
.
Cardiovascular system: Cardio-toxicity is not restricted to
anticancer agents, and almost all therapeutic drug classes have
unanticipated cardio-toxicities. However, cardiotoxicity induced
by chronically administered drugs, such as
neurologic/psychiatric agents and anticancer chemotherapeutic
agents, represents a major problem because toxicity may
become evident only after long-term accumulation of the drug
or its metabolites. Drug-induced cardiotoxicity, commonly in
the form of cardiac muscle dysfunction that may progress to
heart failure, represents a major adverse effect of some common
traditional Antineoplastic agents, e.g., anthracyclines,
cyclophosphamide, 5 fluorouracil, taxanes, as well as newer
agents such as biological monoclonal antibodies, e.g.,
trastuzumab, bevacizumab, and nivolumab; tyrosine kinase
inhibitors, e.g., sunitinib and nilotinib; antiretroviral drugs, e.g.,
zidovudine; antidiabetics, e.g., rosiglitazone; as well as some
illicit drugs such as alcohol, cocaine, methamphetamine,
International Journal of Pharmaceutical Research and Development
www.pharmaceuticaljournal.net
Online ISSN: 2664-6870; Print ISSN: 2664-6862
Received: 02-07-2019; Accepted: 03-08-2019
Volume 1; Issue 2; July 2019; Page No. 06-09

2. International Journal of Pharmaceutical Research and Development
7
ecstasy, and synthetic cannabinoids. Most of the affected
patients had no prior manifestation of the disease [3]
.
Skin: Drug-induced skin disorders are often classified as either
acute or chronic. Acute diseases include erythematous
eruptions; urticaria, angioedema, and anaphylaxis; fixed-drug
eruptions; hypersensitivity syndrome; Stevens-Johnson
syndrome (SJS) and toxic epidermal necrolysis (TEN);
warfarin-induced skin necrosis; vasculitis; serum sickness–like
reaction; acute generalized exanthematous pustulosis (AGEP);
and photosensitivity. Chronic disorders include drug-induced
lupus, drug-induced acne, and pigmentary changes [4]
.
Table 1: Types of drug induced skin disorders
Type Common causative agent
Acute
Erythomatous eruptions penicillins, cephalosporins, sulfonamides, anticonvulsants, and allopurinol
Urticaria, angioedema NSAIDs, antimicrobials, anticancer drugs, ACE inhibitors, corticosteroids.
Fixed-Drug Eruptions Tetracyclines, barbiturates, sulfonamides, codeine, Carbamazepine, acetaminophen, NSAIDs
Drug Hypersensitivity Syndrome Allopurinol, sulfonamides, anticonvulsants, Phenytoin
SJS and TEN Antibacterial sulfonamides, anticonvulsants, nevirapine
Warfarin-Induced Skin Necrosis Warfarin
Serum Sickness–Like Reactions Cefaclor, minocycline, penicillin
AGEP Aminopenicillin, macrolides, quinolones
Photosensitivity Quinolones, Amiodarone, psoralens, Antineoplastic agents
Chronic
Drug-Induced Lupus (DIL):
Drug-Induced Acne (Acneiform Eruption)
Procainamide, hydralazine, quinidine, Isoniazid, chlorpromazine,
TNF inhibitors. Corticosteroids, androgenic hormones, anticonvulsants
Drug-Induced Pigmentary Changes Minocycline, antimalarials, oral contraceptives, imipramine, anticancer drugs.
Neurological conditions: The term neurologic side effect is
commonly used to describe a new drug-induced neurologic
syndrome and/or disorder. Changes in the central nervous
system (brain, spinal cord) or peripheral nerves can cause a
wide variety of symptoms, including loss of coordination and
muscle strength, numbness, loss of consciousness, seizures, and
paralysis (Table 2) [5]
.
Table 2: Drug induced neurological conditions
Lung: The manifestations of drug-induced pulmonary diseases
span the entire spectrum of pathophysiologic conditions of the
respiratory tract. As with most drug-induced diseases, the
pathological changes are nonspecific. Therefore, the diagnosis is
often difficult and, in most cases, is based on exclusion of all
other possible causes. Adverse pulmonary reactions are
uncommon in the general population but are among the most
serious reactions, often requiring intervention. Apnea may be
induced by central nervous system depression or respiratory
neuromuscular blockade. Although the benzodiazepines are
touted as causing less respiratory depression than barbiturates,
they may produce a profound additive or synergistic effect when
taken in combination with other respiratory depressants.
Combining IV diazepam with phenobarbital to stop seizures in

3. International Journal of Pharmaceutical Research and Development
8
an emergency department frequently results in admissions to an
intensive care unit for a short period of assisted mechanical
ventilation, regardless of the drug administration rate. Too rapid
IV administration of any of the benzodiazepines, even without
coadministration of other respiratory depressants, will result in
apnea. Epidemiologic studies demonstrate an increase in the
prevalence of asthma and COPD with increased use
of acetaminophen. The use of aspirin or ibuprofen is not
associated with asthma or COPD. Administration
of acetaminophen in the first year of life was associated with a
46% increase in risk of asthma symptoms at the age of 6 to 7
years. Bronchoconstriction is the most common drug-induced
respiratory problem. Bronchospasm can be induced by a wide
variety of drugs through a number of disparate pathophysiologic
mechanisms. The frequency of aspirin-induced bronchospasm
increases with age, on average at 30 years of age. Both
ethylenediamine tetraacetic acid (EDTA) and benzalkonium
chloride, used as stabilizing and bacteriostatic agents,
respectively, can produce bronchoconstriction. Cough has
become a well-recognized side effect of angiotensin-converting
enzyme (ACE) inhibitor therapy. According to spontaneous
reporting by patients, cough occurs in 1% to 10% of patients
receiving ACE inhibitors, with a preponderance of females. [6]
Gastro-intestinal tract: Medication-induced gastrointestinal
(GI) symptoms and endoscopic pathology are commonly
encountered in clinical practice. Medication-induced GI
disorders may closely mimic other GI conditions (eg, irritable
bowel syndrome (IBS) and inflammatory bowel disease (IBD)),
and failure to recognise drug-related symptoms may lead to
unnecessary investigations and treatment. Medications produce
symptoms by altering GI physiology (eg, constipation induced
by anticholinergic medication), by causing tissue toxicity and
damage (eg, ulcers from non-steroidal anti-inflammatory drugs
(NSAIDs)), by changing the intestinal microbiota (eg,
antibiotics causing Clostridium difficile infection), or by
unknown mechanisms, such as with metformin. The
pharmacologically active compound, as well as the excipient (or
packaging) of the tablet or capsule can cause problems. Nausea
and vomiting may be caused by mechanisms remote from the GI
tract [7, 2]
.
Table 3: Drugs which causes GIT adverse effects
Conditions Drug responsible
Dyspepsia Taxanes, NSAIDs
Acute esophagitis Tetracyclines, bisphosphates.
Reactive gastropathy NSAIDs
Peptic ulcer NSAIDs, corticosteroids
Granulomatous (in stomach) Lanthanum carbonate
Acute gastritis Resins
IBD Rituximab, TNF inhibitors, NSAIDs
Colitis
Sodium phosphate, PPI’s, statins,
colchicines
Ischemia
Digitalis, ergotamine, cocaine, oxygen
peroxide.
Kidney: Drug-induced nephrotoxicity is a common problem in
clinical medicine and the incidence of drug-related acute kidney
injury (AKI) may be as high as 60 percent. Drugs can cause
nephrotoxicity by altering intraglomeu- lar hemodynamics and
decreasing GFR (ACEI, angiotensin-converting enzyme
blockers [ARBs], NSAID, cyclo- sporine, and tacrolimus).
Certain drugs such as ampicillin, ciprofloxacin, sulfon- amides,
acyclovir, ganciclovir, methotrexate and triam- terene are
associated with crystal nephropathy. Statins and alcohol may
induce rhabdomyolysis because of a toxic effect on myocyte
function. Drugs associated with tubular cell toxicity and acute
in- terstitial nephropathy include aminoglycosides, ampho-
tericin B, cisplatin, beta lactams, quinolones, rifampin,
sulfonamides, vancomycin, acyclovir, and contrast agents.
Chronic use of acetaminophen, aspirin, di- uretics and lithium is
associated with chronic interstitial nephritis leading to fibrosis
and renal scarring [8]
.
Blood: The incidence of idiosyncratic drug-induced
hematologic disorders varies depending on the condition and the
associated drug. Few epidemiologic studies have evaluated the
actual incidence of these adverse reactions, but these reactions
appear to be rare. Drugs can produce anaemia by reducing the
production of red blood cells by the bone marrow (e.g.
chloramphenicol, sulfonamides and carbamazepine), or
destroying the formed red blood cells by a process called
hemolysis (e.g. primaquine, penicillin and sulfonamides).
Hemolysis is particularly a problem in patients with the
deficiency of an enzyme called glucose-6-phosphatase. Some
drugs reduce white blood cell counts and increase the chances of
suffering from infections. These include methimazole,
phenylbutazone and clozapine. Heparin has been associated
with thrombocytopenia, a condition that lowers the platelet
counts in the blood and increases the chances of bleeding [9]
.
Bone: Drugs can cause accelerated bone loss as well as
disturbances in serum calcium levels. Long-term use of
glucocorticoids can weaken bones causing osteoporosis and
increasing the risk of fractures. The anti-tubercular drugs
ethambutol and pyrazinamide can increase the blood uric acid,
causing a gout-like disease [10]
.
3. Diagnosis of DIDs
Drug-induced diseases are primarily diagnosed based on the
history of drug intake obtained from the patient or the family.
The symptoms should appear at a reasonable time frame after
taking the medication. By default, physicians should enquire
about drug intake to any patient coming to the clinic with a
problem so as not to miss out on a drug-induced disease. If the
drug is re-administered the symptoms may reappear. This is
referred to as re-challenge. Re-challenge confirms a drug-
induced disease, but is usually not done due to ethical reasons
[2]
.
4. Treatment of DIDs: The first step in the treatment of drug-
induced diseases is to report the adverse effect to the physician
who may stop the intake of the medication or at times, reduce
the dose gradually, and replace with an appropriate alternative.
Many times, this simple step can relieve the patient of the
symptoms. Those who do not recover require additional
treatments depending on the adverse event [2]
.
5. Prevention of DIDs
Steps that could help to prevent a drug-induced disease include
the following:

4. International Journal of Pharmaceutical Research and Development
9
 Always inform your doctor if you suffer from any illness or
take any other medication including a nutritional
supplement before you are prescribed a medication.
 Inform your doctor if you have suffered from any previous
allergic reaction to a drug or any other substances like food
ingredients.
 Take the medication only as prescribed by the doctor. Stick
to the dose, duration of treatment as well as other
instructions like taking it after meals [2]
.
6. Conclusion
Iatrogenic disease or drug induced disease (DID) is an ever
enduring concern for patients, healthcare professionals and
health administrators. In spite of being a major concern in
clinical practice, DID has not been given the due attention it
deserves. One of the reasons for this may be that DID causes
apprehension among health care professionals making them
uncomfortable as well as unwilling to be part of studies
undertaken to reduce DID. In India, several individual case
reports have been published related to specific iatrogenic
disease but a comprehensive study on this problem is not yet
published. The true incidence or prevalence of DID in our
country is not known.
The magnitude of adverse drug reactions which includes DID is
huge. Considering its importance, the Central Drugs Standard
Control Organization (CDSCO), New Delhi, Government of
India, had initiated a nation-wide pharmacovigilance
programme of India (PvPI) in July 2010. The total number of
Individual Case Safety Reports (ICSR) in PvPI database is
84,470. In the US, it was reported that ADRs accounts for more
than one lakh death each year and it is between the fourth and
sixth leading cause of death. In our country, we do not have
statistics on DID but the total ADRs in PvPI database for the
last few years are less than one lakh. This indicates the scenario
of under reporting of ADRs in our country compared to United
States of America.
The various factors contributing to DID can be related to
pharmacokinetic and pharmacodynamic of drugs, non-
adherence to prescribed drug therapy as well as medication
errors. Concurrent diseases (e.g. liver and renal impairments),
genetic polymorphisms in drug metabolizing enzymes and
transporters, nutritional factors (hypo-albuminaemia may result
in more free drug of highly protein bound drugs) and
concomitantly administered drugs may also contribute to
alteration in drug metabolism as well as target receptor activities
of drugs. Hence in this era of personalized medicine, prescribers
need to understand and update their knowledge on the rapidly
transforming drug information. The acquaintance of
pharmacokinetic and pharmacodynamic knowledge of a drug
can help to prevent the DID. Moreover, a good understanding of
pharmaceutical formulations and their applications can help in
reducing DID.
Being on the front lines of patient care as well as
pharmacotherapy, healthcare professionals need to be
knowledgeable regarding the risk of drug-induced diseases,
including methods of detection, prevention, and management.
To be more efficient, health care practitioners need to be skillful
in patient consultation and education in addition to possessing
knowledge on complex biomedical science.
The WHO -UMC (Uppsala Monitoring Centre) Global drug
safety database for the year 2013 has 8.5 million ADR reports.
In this, India’s contribution accounts for nearly 0.7 per cent of
the global data base. In the last 30 years, India has witnessed
banning or withdrawal of nearly 90 drugs for manufacture and
sale by CDSCO (Central Drugs Standard Control Organization).
This forecasts the urgent need to expand the countrywide PvPI
activities so as to implement safety decisions and policy at the
regulatory levels in the interest of patient safety. Policy
decisions regarding patient safety and medication errors can be
achieved through promotion of population based surveillance of
DIDs by PvPI in association with CDSCO. In addition,
continuing medical educational programmes and training need
to be imparted on the healthcare professionals to keep them
updated about DIDs as well as on the measures taken to prevent
them. The importance of spontaneous reporting of adverse drug
reaction needs to be included in the curriculum of all healthcare
professionals and the habit needs to be cultivated right from the
undergraduate level. While doing so care should be taken to
maintain confidentiality of the patients as well as reporting
personals so as to encourage further reporting. Likewise during
diagnosis as well as while teaching medical graduates, emphasis
needs to be given on deliberation of DID as one of the causes of
the disease. Basic and epidemiological researchers interested in
evidence based medicine and personalized medicine can be
motivated to contribute towards the detection, quantification and
reduction of DIDs of the marketed drugs. In addition, carrying
out systematic reviews as well as meta-analysis to generate
evidence towards the occurrence of DID can add required
information to the armamentarium of pharmacovigilance.
7. References
1. Suma TK. drug induced diseases. API 2017; 79:435-438.
2. Dr. Simi Paknikar, Drug Induced Diseases. Med India
medical review. 2017.
3. Kelleni MT, Mahrous AB, Drug Induced Cardiotoxicity:
Mechanism, Prevention and Management, Cardiotoxicity,
Intech Open, 2018.
4. Clinard V, Jennifer DS. US Pharm. 2012; 37(4):HS11-
HS18
5. Demler TL, Drug-Induced Neurologic Conditions. US
Pharm. 2014; 39(1):47-51.
6. Raissy, Hengameh H., Michelle Harkins. "eChapter 15.
Drug-Induced Pulmonary Diseases." Pharmacotherapy: A
Pathophysiologic Approach, 9e Eds. Joseph T. DiPiro, et
al. New York, NY: McGraw-Hill, 2014.
7. Philpott, HL, Nandurkar S, Lubel J, Gibson PR. Drug-
induced gastrointestinal disorders. Frontline
gastroenterology. 2014 5(1):49–57.
8. Ghane SF, Assadi F. Drug-induced renal disorders. Journal
of renal injury prevention. 2015; 4(3):57-60.
9. Rao KV, Chapter 24. Drug-Induced Hematologic
Disorders. In: DiPiro JT, Talbert RL, Yee GC, Matzke GR,
Wells BG, Posey L. eds. Pharmacotherapy: A
Pathophysiologic Approach, 9e New York, NY: McGraw-
Hill, 2014.
10. Bohannon AD, Lyles KW. Drug-induced bone disease. Clin
Geriatr Med. 1994; 10(4):611-23.